via Workday
$90K - 130K a year
Support new product and process introductions by developing manufacturing processes, ensuring quality and compliance, conducting validations, and training manufacturing teams.
Bachelor's degree in engineering with 2+ years relevant experience, preferably in industrial or systems engineering, with knowledge of manufacturing processes, Lean Six Sigma certification preferred, and experience in FDA or regulated industries.
Work Flexibility: Hybrid Stryker’s Sustainability Solutions Advanced Operations team is seeking to hire a Senior Process Engineer, Advanced Operations to work on new product introduction process development in Tempe, AZ. This role supports the execution of assigned project elements with an emphasis on the manufacturing process, technology, and procedures required for the manufacture of new products. What you will do- Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures Ensure quality of process and product as defined in the appropriate operation and material specifications Assist in the selection and design of equipment based on analysis of specifications, reliability, and regulatory requirements Support capital acquisition activities, including specifying equipment, contract negotiation, installation, and validation Write operations manuals, troubleshooting manuals, continuous and preventive maintenance manuals Analyze equipment to establish operating data and conduct experimental test and result analysis Use engineering techniques to reduce product time to market while adhering to regulatory requirements, project deadlines and product costs Participate in process review meetings Participate in process failure mode and effect analysis (PFMEA), control plan, standard operating procedures (SOP) and production part approval process (PPAP) generation associated with product transfers and launches Complete capability studies for in-process inspection and generate subsequent inspection documentation Conduct qualifications, validations, and measurement system analysis (MSA) studies for new products and new processes. Review and approve validation documentation Work in a hands-on manner at the manufacturing site to support the implementation of new processes as specified in development Drive and execute effective communication with all stakeholders to enable project success Provide training for manufacturing team members Ensure adherence to GMP and safety procedures What you need- 2+ years of relevant work experience – required Bachelor’s degree in engineering – required Bachelor's degree in Industrial or Systems Engineering – highly preferred Lean Six Sigma Green Belt Certification or above – preferred Knowledge of manufacturing processes, materials, product, and process design – preferred Good understanding of design for manufacturing (DFM), related statistical tools, and validation/verification techniques – preferred Experience writing and executing validations – preferred Experience in new product introduction or manufacturing engineering – preferred Experience in an FDA regulated or regulated industry – preferred Travel Percentage: 10% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.
This job posting was last updated on 12/10/2025